Phenylpyrimidines
Phenylpyrimidines are a class of organic compounds characterized by the presence of a pyrimidine ring fused to a phenyl group. These molecules find applications in various fields due to their unique chemical properties and structural flexibility. Chemically, phenylpyrimidines possess aromatic rings that enhance their stability and reactivity. They exhibit a range of biological activities, including potential use as antiviral, antibacterial, and anti-inflammatory agents. In pharmaceutical research, these compounds are often investigated for their ability to modulate specific cellular pathways and inhibit various enzymes, making them valuable tools in drug discovery. Additionally, phenylpyrimidines are explored for their potential applications in agrochemicals and materials science, due to their favorable interactions with proteins and nucleic acids.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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2,6-dichloro-4-phenylquinazoline | 5185-54-6 | C14H8Cl2N2 |
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4H-Pyrido[1,2-a]pyrimidin-4-one, 6-methyl-2-phenyl- | 64194-18-9 | C15H12N2O |
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4H-Pyrido[1,2-a]pyrimidin-4-one, 6,7,8,9-tetrahydro-9-methyl-2-phenyl- | 58554-02-2 | C15H16N2O |
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6-(4-chlorophenyl)-2-sulfanylidene-1,2,3,4-tetrahydropyrimidin-4-one | 36479-17-1 | C10H7ClN2OS |
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Methanesulfonamide,N-[5-bromo-4-(4-fluorophenyl)-6-(1-methylethyl)-2-pyrimidinyl]-N-methyl- | 894787-92-9 | C15H17BrFN3O2S |
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N-4-(4-Fluorophenyl)-5-(1E)-3-hydroxy-1-propen-1-yl-6-(1-methylethyl)-2-pyrimidinyl-N-methyl-methanesulfonamide | 910867-08-2 | C18H22FN3O3S |
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Rosuvastatin Calcium | 147098-20-2 | C44H54CaF2N6O12S2 |
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Rosuvastatin methyl ester | 147118-40-9 | C23H30FN3O6S |
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4-(2-Aminopyrimidin-5-yl)benzoic acid | 222987-21-5 | C11H9N3O2 |
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Bropirimine | 56741-95-8 | C10H8BrN3O |
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